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Fig.3.UV-VisabsorptionspectraofsilvernanoparticlesobtainedinthepresenceofHPafterdifferentirradiationtime.(a)0h;(b)4h;(c)24hand(d)36h.
Fig.4.UV-Visabsorptionspectraofsilvernanoparticlesobtainedintheabsence(a)andpresence(b)ofHPafter36hirradiationtime.
wavelengths(blueshift).ThiseffectmaybeexplainedbytheincreasingelectrondensityonthesilverparticlesduetoalterationoftheFermilevel[18].
Incontrast,theAgNO3solutionintheabsenceofHPwasirradiatedinthesameconditions(Fig.4),butnocolorationandabsorptionbandcharacteristicofsurfaceplasmonreso-nancewereobserved.ItwasconceivablethatHPplayedakeyroleinthephotochemicalreductionofAg+.ItmaybeduetothecoordinationbetweenHPandAg+,whichmaydecreasethepotentialofAg+/Ag(EAg+/Ag)andpromotethereductionofAg+.3.4.FT-IRspectra
Tofurthercon rmtheinteractionbetweenHPandAg+,theinfraredspectraweremeasured.AscouldbeseeninFig.5,theabsorptionC=Ostretchingpeakof
HP
at1719cm 1shiftedto1715cm 1aftertheadditionofAgNO3,indicatingthattherewascoordinationbetweenHPandAg+.4.Conclusion
ThisworkpresentedanHP-assistedphotochemicalmethodforproducingsilvernanoparticlesbymeansofUVirradiation.X-raydiffractionresultsshowedthatapureface-centeredcubicsilverphasewasobtainedintheas-preparednanoparticles.TEManalysisshowedthatsilvernanoparticleswerehomogeneouslydispersedinHPmatrix.IntheUV-Visabsorptionspectraoftheobtainednanopar-ticles,theabsorptionpeakduetothesurfaceplasmonreso-nanceofsilverparticleswasobservedatabout430nm.HPwasfoundtoplayakeyroleinthephotochemicalreductionofsilverionsandtheformationofnanosizedparticles.
Fig.5.FT-IRtransmittancespectraofpureHP(a)andAg+-dopedHP
(b).